| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-97662-100ug | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NB100-64803-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-52645-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-82790-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-86935-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-38538-20ul | |||
![Flow Cytometry: LAG-3 Antibody (11E3) [NBP1-97662] - Analysis of 10^6 MCF-7 cells stained using LAG-3 (human) monoclonal antibody (11E3) at a concentration of 50ug/mL.](http://images.novusbio.com/fullsize/LAG-3-Antibody-11E3-Flow-Cytometry-NBP1-97662-img0001.jpg "Flow Cytometry: LAG-3 Antibody (11E3) [NBP1-97662] - Analysis of 10^6 MCF-7 cells stained using LAG-3 (human) monoclonal antibody (11E3) at a concentration of 50ug/mL.")
![Flow Cytometry: CD46 Antibody (MEM-258) [NB500-301] - Staining of human peripheral blood cells with anti-CD46 (MEM-258) Alexa Fluor® 700.](http://images.novusbio.com/fullsize/CD46-Antibody-MEM-258-Flow-Cytometry-NB500-301-img0006.jpg "Flow Cytometry: CD46 Antibody (MEM-258) [NB500-301] - Staining of human peripheral blood cells with anti-CD46 (MEM-258) Alexa Fluor® 700.")
![Flow Cytometry: CD46 Antibody (MEM-258) [NB500-301] - Surface staining of human peripheral blood cells with anti-CD46 (MEM-258) PE](http://images.novusbio.com/fullsize/CD46-Antibody-MEM-258-Flow-Cytometry-NB500-301-img0001.jpg)
![Flow Cytometry: CD46 Antibody (MEM-258) [NB500-301] - Surface staining of human peripheral blood cells with anti-CD46 (MEM-258) biotin](http://images.novusbio.com/fullsize/CD46-Antibody-MEM-258-Flow-Cytometry-NB500-301-img0002.jpg)
![Flow Cytometry: CD46 Antibody (MEM-258) [NB500-301] - Staining of human peripheral blood cells with anti-CD46 (MEM-258) Pacific BlueTM.](http://images.novusbio.com/fullsize/CD46-Antibody-MEM-258-Flow-Cytometry-NB500-301-img0003.jpg)
![Flow Cytometry: CD46 Antibody (MEM-258) [NB500-301] - Staining of human peripheral blood cells with anti-CD46 (MEM-258) APC.](http://images.novusbio.com/fullsize/CD46-Antibody-MEM-258-Flow-Cytometry-NB500-301-img0004.jpg)
![Flow Cytometry: CD46 Antibody (MEM-258) [NB500-301] - Staining of human peripheral blood cells with anti-CD46 (MEM-258) FITC.](http://images.novusbio.com/fullsize/CD46-Antibody-MEM-258-Flow-Cytometry-NB500-301-img0005.jpg)
![Immunohistochemistry-Paraffin: Myeloperoxidase/MPO Antibody (2C7) [NB100-64803] - Mouse anti Human Myeloperoxidase.](http://images.novusbio.com/fullsize/Myeloperoxidase-MPO-Antibody-2C7-Immunohistochemistry-Paraffin-NB100-64803-img0002.jpg "Immunohistochemistry-Paraffin: Myeloperoxidase/MPO Antibody (2C7) [NB100-64803] - Mouse anti Human Myeloperoxidase.")
![Flow Cytometry: Myeloperoxidase/MPO Antibody (2C7) [NB100-64803] - An intracellular stain was performed on Jurkat cells with Myeloperoxidase antibody (2C7) NB100-64803PCP (blue) and a matched isotype control NBP2-27287PCP (orange). Cells were fixed with 4% PFA and then permeablized with 0.1% saponin. Cells were incubated in an antibody dilution of 5 ug/mL for 30 minutes at room temperature. Both antibodies were conjugated to Peridinin-Chlorophyll-Protein complex.](http://images.novusbio.com/fullsize/Myeloperoxidase-MPO-Antibody-2C7-Flow-Cytometry-NB100-64803-img0005.jpg)
![Flow Cytometry: Myeloperoxidase/MPO Antibody (2C7) [NB100-64803] - Staining of human peripheral blood granulocytes with Mouse anti Human myeloperoxidase following permeabilisation with Leucoperm.](http://images.novusbio.com/fullsize/Myeloperoxidase-MPO-Antibody-2C7-Flow-Cytometry-NB100-64803-img0003.jpg)
![Flow Cytometry: Myeloperoxidase/MPO Antibody (2C7) [NB100-64803] - Analysis using the FITC conjugate of NB100-64803. Staining of permeabilised human peripheral blood granulocytes.](http://images.novusbio.com/fullsize/Myeloperoxidase-MPO-Antibody-2C7-Flow-Cytometry-NB100-64803-img0004.jpg)
![Immunocytochemistry/Immunofluorescence: Clusterin/APOJ Antibody [NBP1-06027] - Immunofluorescence analysis of paraformaldehyde fixed PC12 suspension cells, permeabilized with 0.15% Triton. Primary incubation 1hr (10ug/ml) followed by Alexa Fluor 488 secondary antibody (2ug/ml), showing membrane and cytoplasmic staining. The nuclear stain is DAPI (blue). Negative control: Unimmunized goat IgG (10ug/ml) followed by Alexa Fluor 488 secondary antibody (2ug/ml).](http://images.novusbio.com/fullsize/nbp1-06027_goat-polyclonal-clusterin-apoj-antibody-16520239183316.jpg "Immunocytochemistry/Immunofluorescence: Clusterin/APOJ Antibody [NBP1-06027] - Immunofluorescence analysis of paraformaldehyde fixed PC12 suspension cells, permeabilized with 0.15% Triton. Primary incubation 1hr (10ug/ml) followed by Alexa Fluor 488 secondary antibody (2ug/ml), showing membrane and cytoplasmic staining. The nuclear stain is DAPI (blue). Negative control: Unimmunized goat IgG (10ug/ml) followed by Alexa Fluor 488 secondary antibody (2ug/ml).")
![Western Blot: Clusterin/APOJ Antibody [NBP1-06027] - (0.1ug/ml) staining of Mouse (A) and (0.3ug/ml) Rat (B) Brain lysate (35ug protein in RIPA buffer). Detected by chemiluminescence.](http://images.novusbio.com/fullsize/nbp1-06027_goat-polyclonal-clusterin-apoj-antibody-1652023918330.jpg)
![Immunocytochemistry/Immunofluorescence: Complement C3 Antibody (JF10-30) [NBP2-66994] - Staining C3 in NIH/3T3 cells (red). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X-100, PBS.](http://images.novusbio.com/fullsize/Complement-C3-Antibody-JF10-30-Immunocytochemistry-Immunofluorescence-NBP2-66994-img0002.jpg "Immunocytochemistry/Immunofluorescence: Complement C3 Antibody (JF10-30) [NBP2-66994] - Staining C3 in NIH/3T3 cells (red). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X-100, PBS.")
![Flow Cytometry: Complement C3 Antibody (JF10-30) [NBP2-66994] - Analysis of HepG2 cells with C3 antibody at 1:50 dilution (red) compared with an unlabelled control (cells without incubation with primary antibody; black). Alexa Fluor 488-conjugated goat anti rabbit IgG was used as the secondary antibody](http://images.novusbio.com/fullsize/Complement-C3-Antibody-JF10-30-Flow-Cytometry-NBP2-66994-img0001.jpg)
![Flow Cytometry: Complement C3 Antibody (JF10-30) [NBP2-66994] - Cells were fixed and permeabilized. Then stained with the primary antibody (1μg/mL) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4c for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody (HA1121) at 1/1,000 dilution for 30 minutes at +4 c. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).](http://images.novusbio.com/fullsize/nbp2-66994_rabbit-monoclonal-complement-c3-antibody-jf10-30-flow-cytometry-1542024105623..jpg)
![Western Blot: Complement C3 Antibody (JF10-30) [NBP2-66994] -Western blot analysis of C3 on different lysates with Rabbit anti-C3 antibody at 1/1,000 dilution.Lane 1: Human liver tissue lysateLane 2: HepG2 cell lysateLane 3: HeLa cell lysateLane 4: Mouse liver tissue lysateLane 5: Mouse spleen tissue lysateLane 6: Rat liver tissue lysateLane 7: Rat spleen tissue lysateLysates/proteins at 30 µg/Lane.Predicted band size: 187 kDaObserved band size: 108/37 kDaExposure time: 1 minute;4-20% SDS-PAGE gel.](http://images.novusbio.com/fullsize/nbp2-66994_rabbit-monoclonal-complement-c3-antibody-jf10-30-western-blot-1542024105739..jpg)
![Immunocytochemistry/Immunofluorescence: Complement C3 Antibody (JF10-30) [NBP2-66994] -Cells were fixed in 100% precooled methanol for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-C3 antibody at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI.Beta tubulin (M1305-2, red) was stained at 1/100 dilution overnight at +4 c. Goat Anti-Mouse IgG H&L (iFluor™ ) was used as the secondary antibody at 1/1,000 dilution.](http://images.novusbio.com/fullsize/nbp2-66994_rabbit-monoclonal-complement-c3-antibody-jf10-30-immunocytochemistry-immunofluorescence-15420241102..jpg)
![Dual RNAscope ISH-IHC: CD52 Antibody (Campath-1H) [NBP2-52645] - Formalin-fixed paraffin-embedded tissue sections of human tonsil were probed for CD52 mRNA (ACD RNAScope probe, catalog # 519381; Fast Red chromogen, ACD catalog # 322500) followed by immunohistochemistry using rabbit monoclonal (Novus catalog # NBP2-52645) at 5ug/mL for 1 hour at room temperature and detection with anti-mouse IgG VisUCyte HRP Polymer Antibody (R&D Systems Catalog # VC003) and green HRP chromogen (ACD Catalog # 322500).](http://images.novusbio.com/fullsize/CD52-Antibody-Campath-1H-Dual-RNAscope-ISH-IHC-NBP2-52645-img0010.jpg "<b>Orthogonal Strategies Validation. </b>Dual RNAscope ISH-IHC: CD52 Antibody (Campath-1H) [NBP2-52645] - Formalin-fixed paraffin-embedded tissue sections of human tonsil were probed for CD52 mRNA (ACD RNAScope probe, catalog # 519381; Fast Red chromogen, ACD catalog # 322500) followed by immunohistochemistry using rabbit monoclonal (Novus catalog # NBP2-52645) at 5ug/mL for 1 hour at room temperature and detection with anti-mouse IgG VisUCyte HRP Polymer Antibody (R&D Systems Catalog # VC003) and green HRP chromogen (ACD Catalog # 322500).")
![<b>Orthogonal Strategies Validation. </b>Flow Cytometry: CD52 Antibody (Campath-1H) [NBP2-52645] - Flow-cytometry using anti-CD52 antibody Campath-1H. Cynomolgus monkey lymphocytes were stained with an isotype control (panel A) or the rabbit-chimeric version of Campath-1H (panel B) at a concentration of 1 ug/ml for 30 mins at RT. After washing, bound antibody was detected using a AF488 conjugated donkey anti-rabbit antibody and cells analysed on a FACSCanto flow-cytometer.](http://images.novusbio.com/fullsize/CD52-Antibody-Campath-1H-NBP2-52645-img0005.jpg)
![Flow Cytometry: CD52 Antibody (Campath-1H) [NBP2-52645] - Flow-cytometry using anti-CD52 antibody Campath-1H. Rhesus monkey lymphocytes were stained with an isotype control (panel A) or the rabbit-chimeric version of Campath-1H (panel B) at a concentration of 1 ug/ml for 30 mins at RT. After washing, bound antibody was detected using a AF488 conjugated donkey anti-rabbit antibody and cells analysed on a FACSCanto flow-cytometer.](http://images.novusbio.com/fullsize/CD52-Antibody-Campath-1H-NBP2-52645-img0004.jpg)
![Immunohistochemistry-Paraffin: CD46 Antibody [NBP1-82790] - Analysis in human placenta and pancreas tissues. Corresponding CD46 RNA-seq data are presented for the same tissues.](http://images.novusbio.com/fullsize/CD46-Antibody-Immunohistochemistry-Paraffin-NBP1-82790-img0009.jpg "<b>Orthogonal Strategies Validation. </b>Immunohistochemistry-Paraffin: CD46 Antibody [NBP1-82790] - Analysis in human placenta and pancreas tissues. Corresponding CD46 RNA-seq data are presented for the same tissues.")
![<b>Orthogonal Strategies Validation. </b>Western Blot: CD46 Antibody [NBP1-82790] - Analysis in control (vector only transfected HEK293T lysate) and CD46 over-expression lysate (Co-expressed with a C-terminal myc-DDK tag (3.1 kDa) in mammalian HEK293T cells).](http://images.novusbio.com/fullsize/CD46-Antibody-Western-Blot-NBP1-82790-img0008.jpg)
![Immunohistochemistry-Paraffin: CD46 Antibody [NBP1-82790] - Staining of human prostate shows moderate membranous positivity in glandular cells.](http://images.novusbio.com/fullsize/CD46-Antibody-Immunohistochemistry-Paraffin-NBP1-82790-img0013.jpg)
![Immunohistochemistry-Paraffin: CD46 Antibody [NBP1-82790] - Staining of human endometrium shows weak membranous positivity in glandular cells.](http://images.novusbio.com/fullsize/CD46-Antibody-Immunohistochemistry-Paraffin-NBP1-82790-img0010.jpg)
![Immunohistochemistry-Paraffin: CD46 Antibody [NBP1-82790] - Staining of human pancreas shows no positivity in a subset of exocrine glandular cells as expected.](http://images.novusbio.com/fullsize/CD46-Antibody-Immunohistochemistry-Paraffin-NBP1-82790-img0011.jpg)
![Immunohistochemistry-Paraffin: CD46 Antibody [NBP1-82790] - Staining of human placenta shows moderate membranous positivity in trophoblastic cells.](http://images.novusbio.com/fullsize/CD46-Antibody-Immunohistochemistry-Paraffin-NBP1-82790-img0012.jpg)
![Immunohistochemistry-Paraffin: Serpin G1/C1 Inhibitor Antibody (HL1196) - Azide and BSA Free [NBP3-25387] - C1 inhibitor antibody [HL1196] detects secreted C1 inhibitor protein by immunohistochemical analysis. Sample: Paraffin-embedded human breast carcinoma. C1 inhibitor stained by C1 inhibitor antibody [HL1196] (NBP3-25387) diluted at 1:100. Antigen Retrieval: Citrate buffer, pH 6.0, 15 min](http://images.novusbio.com/fullsize/nbp3-25387_rabbit-serpin-g1-c1-inhibitor-mab-hl1196-azide-bsa-free-2120249432810.jpg "Immunohistochemistry-Paraffin: Serpin G1/C1 Inhibitor Antibody (HL1196) - Azide and BSA Free [NBP3-25387] - C1 inhibitor antibody [HL1196] detects secreted C1 inhibitor protein by immunohistochemical analysis. Sample: Paraffin-embedded human breast carcinoma. C1 inhibitor stained by C1 inhibitor antibody [HL1196] (NBP3-25387) diluted at 1:100. Antigen Retrieval: Citrate buffer, pH 6.0, 15 min")
![Immunohistochemistry-Paraffin: Serpin G1/C1 Inhibitor Antibody (HL1196) - Azide and BSA Free [NBP3-25387] - C1 inhibitor antibody [HL1196] detects C1 inhibitor protein by immunohistochemical analysis. Sample: Paraffin-embedded rat tissues. C1 inhibitor stained by C1 inhibitor antibody [HL1196] (NBP3-25387) diluted at 1:100. Antigen Retrieval: Citrate buffer, pH 6.0, 15 min](http://images.novusbio.com/fullsize/nbp3-25387_rabbit-serpin-g1-c1-inhibitor-mab-hl1196-azide-bsa-free-2120249403885.jpg)
![Western Blot: Serpin G1/C1 Inhibitor Antibody (HL1196) - Azide and BSA Free [NBP3-25387] - Mouse plasma and rat plasma (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with C1 inhibitor antibody [HL1196] (NBP3-25387) diluted at 1:2000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-25387_rabbit-serpin-g1-c1-inhibitor-mab-hl1196-azide-bsa-free-212024939188.jpg)
![Immunocytochemistry/Immunofluorescence: Serpin G1/C1 Inhibitor Antibody (HL1196) - Azide and BSA Free [NBP3-25387] - C1 inhibitor antibody [HL1196] detects C1 inhibitor protein by immunofluorescent analysis. Sample: HepG2 cells were fixed in ice-cold MeOH for 10 min. Green: C1 inhibitor stained by C1 inhibitor antibody [HL1196] (NBP3-25387) diluted at 1:500. Blue: Fluoroshield with DAPI .](http://images.novusbio.com/fullsize/nbp3-25387_rabbit-serpin-g1-c1-inhibitor-mab-hl1196-azide-bsa-free-2120249393589.jpg)
![Western Blot: Serpin G1/C1 Inhibitor Antibody (HL1196) - Azide and BSA Free [NBP3-25387] - Human plasma (30 ug) was separated by 10% SDS-PAGE, and the membrane was blotted with C1 inhibitor antibody [HL1196] (NBP3-25387) diluted at 1:10000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-25387_rabbit-serpin-g1-c1-inhibitor-mab-hl1196-azide-bsa-free-2120249374915.jpg)
![Western Blot: Complement Component C1qA Antibody [NBP3-13331] - Rat plasma (30 ug) was separated by 12% SDS-PAGE, and the membrane was blotted with Complement Component C1qA antibody (NBP3-13331) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/Complement-Component-C1qA-Antibody-Western-Blot-NBP3-13331-img0005.jpg "Western Blot: Complement Component C1qA Antibody [NBP3-13331] - Rat plasma (30 ug) was separated by 12% SDS-PAGE, and the membrane was blotted with Complement Component C1qA antibody (NBP3-13331) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.")
![Immunohistochemistry-Paraffin: Complement Component C1qA Antibody [NBP3-13331] - Rat thymus gland. Complement Component C1qA stained by Complement Component C1qA antibody (NBP3-13331) diluted at 1:2000. Antigen Retrieval: Citrate buffer, pH 6.0, 15 min.](http://images.novusbio.com/fullsize/Complement-Component-C1qA-Antibody-Immunohistochemistry-Paraffin-NBP3-13331-img0002.jpg)
![Western Blot: Complement Component C1qA Antibody [NBP3-13331] - Mouse plasma (50 ug) was separated by 12% SDS-PAGE, and the membrane was blotted with Complement Component C1qA antibody (NBP3-13331) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/Complement-Component-C1qA-Antibody-Western-Blot-NBP3-13331-img0001.jpg)
![Western Blot: Complement Component C1qA Antibody [NBP3-13331] - Human plasma (30 ug) was separated by 12% SDS-PAGE, and the membrane was blotted with Complement Component C1qA antibody (NBP3-13331) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/Complement-Component-C1qA-Antibody-Western-Blot-NBP3-13331-img0004.jpg)
![Immunohistochemistry: CD21 Antibody [NBP3-38538] - Immunohistochemistry analysis of paraffin-embedded Rat spleen using CD21 Rabbit pAb at dilution of 1:100 (40x lens). Microwave antigen retrieval performed with 0.01M PBS Buffer (pH 7.2) prior to IHC staining.](http://images.novusbio.com/fullsize/nbp3-38538_rabbit-cd21-pab-9122024159579.jpg "Immunohistochemistry: CD21 Antibody [NBP3-38538] - Immunohistochemistry analysis of paraffin-embedded Rat spleen using CD21 Rabbit pAb at dilution of 1:100 (40x lens). Microwave antigen retrieval performed with 0.01M PBS Buffer (pH 7.2) prior to IHC staining.")
![Immunocytochemistry/ Immunofluorescence: CD21 Antibody [NBP3-38538] - Immunofluorescence analysis of paraffin-embedded human spleen using CD21 Rabbit pAb at dilution of 1:100 (40x lens). Secondary antibody: Cy3-conjugated Goat anti-Rabbit IgG (H+L) at 1:500 dilution. Blue: DAPI for nuclear staining.](http://images.novusbio.com/fullsize/nbp3-38538_rabbit-cd21-pab-912202415171172.jpg)
![Western Blot: CD21 Antibody [NBP3-38538] - Western blot analysis of various lysates using CD21 Rabbit pAb at 1:1000 dilution.Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25ug per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit.Exposure time: 60s.](http://images.novusbio.com/fullsize/nbp3-38538_rabbit-cd21-pab-912202414163018.jpg)
![Immunocytochemistry/ Immunofluorescence: CD21 Antibody [NBP3-38538] - Immunofluorescence analysis of paraffin-embedded mouse spleen using CD21 Rabbit pAb at dilution of 1:100 (40x lens). Secondary antibody: Cy3-conjugated Goat anti-Rabbit IgG (H+L) at 1:500 dilution. Blue: DAPI for nuclear staining.](http://images.novusbio.com/fullsize/nbp3-38538_rabbit-cd21-pab-912202415121332.jpg)
![Immunocytochemistry/ Immunofluorescence: CD21 Antibody [NBP3-38538] - Immunofluorescence analysis of paraffin-embedded rat spleen using CD21 Rabbit pAb at dilution of 1:100 (40x lens). Secondary antibody: Cy3-conjugated Goat anti-Rabbit IgG (H+L) at 1:500 dilution. Blue: DAPI for nuclear staining.](http://images.novusbio.com/fullsize/nbp3-38538_rabbit-cd21-pab-912202415171157.jpg)